JPS6337157A - 抵抗率が低下した架橋ポリマ−、ならびにそれらを製造するための材料および方法 - Google Patents

抵抗率が低下した架橋ポリマ−、ならびにそれらを製造するための材料および方法

Info

Publication number: JPS6337157A
Authority: JP; Japan
Prior art keywords: polymer; crosslinking; crosslinking agent; crosslinked; agent
Prior art date: 1986-07-30
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Pending

Application number

JP62191474A

Other languages

English (en)

Japanese (ja)

Inventor

ポール・ダニエル・ヤコブッチ

トーマス・アルバノ

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Eastman Kodak Co

Original Assignee

Eastman Kodak Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1986-07-30

Filing date

1987-07-30

Publication date

1988-02-17

1987-07-30 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1988-02-17 Publication of JPS6337157A publication Critical patent/JPS6337157A/ja

Status Pending legal-status Critical Current

Links

239000000463 material Substances 0.000 title claims description 7
229920006037 cross link polymer Polymers 0.000 title description 22
238000004519 manufacturing process Methods 0.000 title description 5
229920000642 polymer Polymers 0.000 claims description 70
239000003795 chemical substances by application Substances 0.000 claims description 46
238000011282 treatment Methods 0.000 claims description 44
239000003431 cross linking reagent Substances 0.000 claims description 36
238000004132 cross linking Methods 0.000 claims description 25
238000000034 method Methods 0.000 claims description 22
125000001453 quaternary ammonium group Chemical group 0.000 claims description 14
239000004971 Cross linker Substances 0.000 claims description 13
150000001875 compounds Chemical class 0.000 claims description 3
239000000203 mixture Substances 0.000 description 25
239000007858 starting material Substances 0.000 description 15
238000009472 formulation Methods 0.000 description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
239000000178 monomer Substances 0.000 description 10
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 8
239000003973 paint Substances 0.000 description 7
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
238000000576 coating method Methods 0.000 description 6
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
125000000524 functional group Chemical group 0.000 description 5
239000002904 solvent Substances 0.000 description 5
BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 description 4
239000011248 coating agent Substances 0.000 description 4
125000001033 ether group Chemical group 0.000 description 4
KFZMGEQAYNKOFK-UHFFFAOYSA-N isopropyl alcohol Natural products CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
239000004408 titanium dioxide Substances 0.000 description 4
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
239000008199 coating composition Substances 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
229920000728 polyester Polymers 0.000 description 3
238000003756 stirring Methods 0.000 description 3
239000012463 white pigment Substances 0.000 description 3
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
239000004925 Acrylic resin Substances 0.000 description 2
229920000178 Acrylic resin Polymers 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000002411 adverse Effects 0.000 description 2
150000008064 anhydrides Chemical group 0.000 description 2
LVPQDMDVCZOHCK-UHFFFAOYSA-M butyl-bis(2-hydroxyethyl)-methylazanium;bromide Chemical compound [Br-].CCCC[N+](C)(CCO)CCO LVPQDMDVCZOHCK-UHFFFAOYSA-M 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
239000006258 conductive agent Substances 0.000 description 2
239000002612 dispersion medium Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000003822 epoxy resin Substances 0.000 description 2
229910052731 fluorine Inorganic materials 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
125000004433 nitrogen atom Chemical group N* 0.000 description 2
239000000049 pigment Substances 0.000 description 2
229920000647 polyepoxide Polymers 0.000 description 2
229920001225 polyester resin Polymers 0.000 description 2
239000004645 polyester resin Substances 0.000 description 2
239000002243 precursor Substances 0.000 description 2
LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 2
230000001681 protective effect Effects 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
229920001187 thermosetting polymer Polymers 0.000 description 2
125000003396 thiol group Chemical class [H]S* 0.000 description 2
239000008096 xylene Substances 0.000 description 2
MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 description 1
229940093475 2-ethoxyethanol Drugs 0.000 description 1
125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
YEYKMVJDLWJFOA-UHFFFAOYSA-N 2-propoxyethanol Chemical compound CCCOCCO YEYKMVJDLWJFOA-UHFFFAOYSA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
235000004391 Chenopodium capitatum Nutrition 0.000 description 1
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 1
241000167766 Lithospermum canescens Species 0.000 description 1
206010067482 No adverse event Diseases 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical group 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
ULOMEYHCTBRGAQ-UHFFFAOYSA-M decyl-bis(2-hydroxyethyl)-methylazanium;bromide Chemical compound [Br-].CCCCCCCCCC[N+](C)(CCO)CCO ULOMEYHCTBRGAQ-UHFFFAOYSA-M 0.000 description 1
150000002118 epoxides Chemical class 0.000 description 1
CJMZLCRLBNZJQR-UHFFFAOYSA-N ethyl 2-amino-4-(4-fluorophenyl)thiophene-3-carboxylate Chemical compound CCOC(=O)C1=C(N)SC=C1C1=CC=C(F)C=C1 CJMZLCRLBNZJQR-UHFFFAOYSA-N 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
239000002923 metal particle Substances 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000005012 migration Effects 0.000 description 1
238000013508 migration Methods 0.000 description 1
238000002156 mixing Methods 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920005862 polyol Polymers 0.000 description 1
150000003077 polyols Chemical class 0.000 description 1
DGMKFQYCZXERLX-UHFFFAOYSA-N proglumide Chemical compound CCCN(CCC)C(=O)C(CCC(O)=O)NC(=O)C1=CC=CC=C1 DGMKFQYCZXERLX-UHFFFAOYSA-N 0.000 description 1
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
238000002310 reflectometry Methods 0.000 description 1
229920006009 resin backbone Polymers 0.000 description 1
239000010959 steel Substances 0.000 description 1
-1 trimethylolpropane Chemical class 0.000 description 1
239000002966 varnish Substances 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L67/00—Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C08K5/19—Quaternary ammonium compounds
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Paints Or Removers (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Processes Of Treating Macromolecular Substances (AREA)
Compositions Of Macromolecular Compounds (AREA)

JP62191474A 1986-07-30 1987-07-30 抵抗率が低下した架橋ポリマ−、ならびにそれらを製造するための材料および方法 Pending JPS6337157A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US06/892,173 US4698391A (en)	1986-07-30	1986-07-30	Crosslinked polymers with lowered resistivity and materials and methods for their preparation
US892173		1992-06-02

Publications (1)

Publication Number	Publication Date
JPS6337157A true JPS6337157A (ja)	1988-02-17

Family

ID=25399495

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP62191474A Pending JPS6337157A (ja)	1986-07-30	1987-07-30	抵抗率が低下した架橋ポリマ−、ならびにそれらを製造するための材料および方法

Country Status (4)

Country	Link
US (1)	US4698391A (de)
EP (1)	EP0254874A3 (de)
JP (1)	JPS6337157A (de)
CA (1)	CA1277080C (de)

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DE3716861A1 (de) *	1987-05-20	1988-12-15	Flachglas Ag	Aushaertbare up-formmasse mit reduziertem elektrischem oberflaechenwiderstand
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US5011739A (en) *	1989-10-02	1991-04-30	Eastman Kodak Company	Moisture stable biasable transfer members and method for making same
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US5281643A (en) *	1991-05-28	1994-01-25	Istituto Guido Donegani S.P.A.	Thermoplastic polyester molding compositions containing quaternary ammonium compounds
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US5420267A (en) *	1991-08-09	1995-05-30	Eastman Chemical Company	Cellulose acetoacetate esters
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US5218042A (en) *	1991-09-25	1993-06-08	Thauming Kuo	Water-dispersible polyester resins and process for their preparation
US5250357A (en) *	1991-11-26	1993-10-05	Eastman Kodak Company	Moisture stable elastomeric polyurethane biasable transfer members
US5217838A (en) *	1991-11-26	1993-06-08	Eastman Kodak Company	Moisture stable biasable transfer members
US5212032A (en) *	1991-11-26	1993-05-18	Eastman Kodak Company	Moisture stable polyurethane biasable transfer members
US5349010A (en) *	1992-09-30	1994-09-20	Eastman Chemical Company	Water-dispersible polyester resins and process for their preparation
US5322885A (en) *	1992-11-02	1994-06-21	Eastman Chemical Company	Aqueous dispersion compositions and coatings prepared therefrom
US5378757A (en) *	1993-11-15	1995-01-03	Eastman Chemical Company	Water-dissipatable alkyd resins and coatings prepared therefrom
AU7718496A (en)	1995-10-20	1997-05-07	Drexel University	End-functionalized aniline-based oligomers, corrosion-resistant copolymers and methods of making the same
US6333378B1 (en)	1997-08-12	2001-12-25	Eastman Chemical Company	Acrylic modified waterborne alkyd or uralkyd dispersions
DE69831955T2 (de)	1997-08-12	2006-04-27	Eastman Chemical Co., Kingsport	Acrylmodifizierte wässrige sulphonierte alkyddispersionen
EP1194469B1 (de)	1999-06-29	2004-09-15	Eastman Chemical Company	Zwischenprodukt eines polyesterharzes. herstellungsverfahren von diesem zwischenprodukt, zusammensetzung enthaltend dieses produkt, und ihre verwendungen
US20050004272A1 (en) *	2003-06-23	2005-01-06	Thauming Kuo	Small-particle latex compositions based on waterborne alkyd seeds
US20060270769A1 (en) *	2005-05-24	2006-11-30	Shoaf Glenn L	Acrylic-modified alkyd hybrid latexes and their use as viscosity modifiers
CN101768415B (zh) *	2008-12-30	2013-03-27	第一毛织株式会社	抗静电粘合剂组合物、粘合膜及其制备方法
US8168721B2 (en)	2009-02-06	2012-05-01	Eastman Chemical Company	Coating compositions containing tetramethyl cyclobutanediol
US9029461B2 (en) *	2009-02-06	2015-05-12	Eastman Chemical Company	Aliphatic polyester coating compositions containing tetramethyl cyclobutanediol
US8163850B2 (en)	2009-02-06	2012-04-24	Eastman Chemical Company	Thermosetting polyester coating compositions containing tetramethyl cyclobutanediol
US8324316B2 (en) *	2009-02-06	2012-12-04	Eastman Chemical Company	Unsaturated polyester resin compositions containing 2,2,2,4-tetramethyl-1,3-cyclobutanediol and articles made therefrom
US9029460B2 (en)	2009-02-06	2015-05-12	Stacey James Marsh	Coating compositions containing acrylic and aliphatic polyester blends
US9650539B2 (en)	2014-10-27	2017-05-16	Eastman Chemical Company	Thermosetting compositions based on unsaturated polyesters and phenolic resins
US9598602B2 (en)	2014-11-13	2017-03-21	Eastman Chemical Company	Thermosetting compositions based on phenolic resins and curable poleyester resins made with diketene or beta-ketoacetate containing compounds
CN107148433A (zh)	2014-10-27	2017-09-08	伊士曼化工公司	可用官能聚酯固化的甲阶酚醛树脂
US9487619B2 (en)	2014-10-27	2016-11-08	Eastman Chemical Company	Carboxyl functional curable polyesters containing tetra-alkyl cyclobutanediol
US20160340471A1 (en)	2015-05-19	2016-11-24	Eastman Chemical Company	Aliphatic polyester coating compositions containing tetramethyl cyclobutanediol
US20170088665A1 (en)	2015-09-25	2017-03-30	Eastman Chemical Company	POLYMERS CONTAINING CYCLOBUTANEDIOL AND 2,2 BIS(HYDROXYMETHYL) AlKYLCARBOXYLIC ACID
US20170101502A1 (en)	2015-10-13	2017-04-13	Eastman Chemical Company	Systems and methods for forming polyurethanes
US9988553B2 (en)	2016-02-22	2018-06-05	Eastman Chemical Company	Thermosetting coating compositions
US10011737B2 (en)	2016-03-23	2018-07-03	Eastman Chemical Company	Curable polyester polyols and their use in thermosetting soft feel coating formulations
US10687528B2 (en)	2017-12-12	2020-06-23	International Business Machines Corporation	Antimicrobial polymers with enhanced functionalities
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JPS5924727A (ja) *	1982-08-02	1984-02-08	Asahi Chem Ind Co Ltd	活性表面を有する糸、フイルムあるいは成形品及びその製造方法

1986
- 1986-07-30 US US06/892,173 patent/US4698391A/en not_active Expired - Lifetime
1987
- 1987-05-27 CA CA000538066A patent/CA1277080C/en not_active Expired - Fee Related
- 1987-06-25 EP EP87109131A patent/EP0254874A3/de not_active Withdrawn
- 1987-07-30 JP JP62191474A patent/JPS6337157A/ja active Pending

Also Published As

Publication number	Publication date
EP0254874A2 (de)	1988-02-03
CA1277080C (en)	1990-11-27
EP0254874A3 (de)	1990-02-07
US4698391A (en)	1987-10-06

Publication	Publication Date	Title
JPS6337157A (ja)	1988-02-17	抵抗率が低下した架橋ポリマ−、ならびにそれらを製造するための材料および方法
JP3973718B2 (ja)	2007-09-12	耐環境腐食性コーティング用の水性コーティング組成物
CA1236631A (en)	1988-05-10	Process for the preparation of urea condensates and their use
US3849160A (en)	1974-11-19	Coating with pulverulent mixtures of hydroxy containing polymers and {68 -caprolactam masked polyisocyanates
US4971727A (en)	1990-11-20	Conductive primer for plastics or conductive primer surfacer paint and coated plastics molded products
JPS5825388B2 (ja)	1983-05-27	マツタンニカルボキシルキオモツカキヨウザイオフクムフンタイトソウソセイブツ
EP0287877B1 (de)	1995-12-20	Verbundwerkstoff und Verfahren zu dessen Herstellung
JPS6259736B2 (de)	1987-12-12
JPH02305995A (ja)	1990-12-19	複合塗膜
JP2003517369A (ja)	2003-05-27	被覆材料
EP0435356B1 (de)	1994-11-09	Wärmehärtendes Überzugsmittel und Herstellung eines pigmentierten Films
JPH03502816A (ja)	1991-06-27	硬化性組成物、その製法並びにそれよりなるクリアラッカー
JP3191874B2 (ja)	2001-07-23	迅速硬化性の被覆組成物
JP3144332B2 (ja)	2001-03-12	熱架橋性塗料用樹脂組成物およびその用途
JP2986443B2 (ja)	1999-12-06	熱硬化性樹脂組成物及びその硬化方法
JP3246956B2 (ja)	2002-01-15	アクリルアミド系及びメタクリルアミド系カチオン変性共重合体の製造方法
US4877502A (en)	1989-10-31	Poly(epoxide) coatings containing a mannich base of a hydroxystyrene containing polymer
JPH0334783B2 (de)	1991-05-23
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